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Details

Autor(en) / Beteiligte
Titel
Cost effectiveness of therapeutic drug monitoring for imatinib administration in chronic myeloid leukemia
Ist Teil von
  • PloS one, 2019-12, Vol.14 (12), p.e0226552-e0226552
Ort / Verlag
United States: Public Library of Science
Erscheinungsjahr
2019
Link zum Volltext
Quelle
MEDLINE
Beschreibungen/Notizen
  • Imatinib mesylate (IM) is a first-line treatment option for patients with chronic myeloid leukemia (CML). Patients who fail or are intolerant to IM therapy are treated with more expensive second and third-generation tyrosine kinase inhibitors. Patients show wide variation in trough concentrations in response to standard dosing. Thus, many patients receive subtherapeutic or supratherapeutic doses. Therapeutic drug monitoring (TDM) may improve dose management that, in turn, may reduce costs and improve outcomes. However, TDM also adds to the cost of patient care. The objective of this study was to determine the cost-effectiveness of TDM for generic IM therapy. We developed a microsimulation model for the trough plasma concentration of IM which is related to a cytogenetic or molecular response. We compared two cohorts: one with TDM and one without TDM (NTDM). The lifetime incremental cost-effectiveness ratio (ICER) was calculated using quality-adjusted life years (QALYs) as the effectiveness measure. One-way and probabilistic sensitivity analyses were performed. The lifetime cost and QALY of treatment with TDM were $2,137K [95% Ci: 2,079K; 2,174K] and 12.37 [95% CI: 12.07; 12.55], respectively. The cost and QALY of NTDM were $2,132K [95% CI: 2,091K; 2,197K] and 12.23 [95% CI: 11.96; 12.50], respectively. The incremental cost and QALY for TDM relative to NTDM was $4,417 [95% CI: -52,582; 32,097]) and 0.15 [95% CI: -0.13; 0.28]. The ICER for TDM relative to NTDM was $30,450/QALY. Probabilistic sensitivity analysis showed that TDM was cost-effective relative to NTDM in 90% of the tested scenarios at a willingness-to-pay threshold of $100,000/QALY. Although the impact of TDM is modest, the cost-effectiveness over a lifetime horizon (societal perspective, ($30,450/QALY) falls within the acceptable range (< $100k/QALY).
Sprache
Englisch
Identifikatoren
ISSN: 1932-6203
eISSN: 1932-6203
DOI: 10.1371/journal.pone.0226552
Titel-ID: cdi_plos_journals_2330057677
Format
Schlagworte
Analysis, Antimitotic agents, Antineoplastic agents, Antineoplastic Combined Chemotherapy Protocols - economics, Antineoplastic Combined Chemotherapy Protocols - therapeutic use, Biology and Life Sciences, Bosutinib, Chemotherapy, Chronic myeloid leukemia, Computer Simulation, Cost analysis, Cost effectiveness, Cost-Benefit Analysis, Cytogenetic Analysis, Cytogenetics, Dasatinib, Dosage, Drug dosages, Drug Monitoring - economics, Drug Monitoring - methods, Drug Resistance, Neoplasm - genetics, Drug-Related Side Effects and Adverse Reactions - economics, Drug-Related Side Effects and Adverse Reactions - epidemiology, Drug-Related Side Effects and Adverse Reactions - genetics, Drug-Related Side Effects and Adverse Reactions - therapy, Drugs, Generic - economics, Drugs, Generic - therapeutic use, Economic aspects, Generic drugs, Health aspects, Hematopoietic Stem Cell Transplantation - economics, Hematopoietic Stem Cell Transplantation - statistics & numerical data, Humans, Imatinib, Imatinib Mesylate - economics, Imatinib Mesylate - therapeutic use, Inhibitor drugs, Kinases, Laboratories, Leukemia, Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy, Leukemia, Myelogenous, Chronic, BCR-ABL Positive - economics, Leukemia, Myelogenous, Chronic, BCR-ABL Positive - epidemiology, Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics, Medication Adherence - statistics & numerical data, Medicine and Health Sciences, Monitoring, Mutation, Myeloid leukemia, Nilotinib, Pathology, Patients, Pharmacogenomic Testing, Phenols (Class of compounds), Ponatinib, Protein-tyrosine kinase, Quality-Adjusted Life Years, Sensitivity analysis, Social Sciences, Stem cell transplantation, Success, Survival Analysis, Targeted cancer therapy, Therapeutic drug monitoring, Therapy, Tyrosine

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